Synthesis and antimicrobial evaluation with DFT study for new thiazole derivatives

Two compounds,[2-amino-4-(4-nitro phenyl) 1,3-thiazole],(4) and [2-amino-4-(4-bromo phenyl) 1,3-thiazole],(5), were synthesized by refluxing thiourea (1) with each of  para-ntiro and para-bomophanacyl bromides(2) and (3) respectively, in absolute methanol. Then, by reaction of [5] with 3,5-dinitrob...

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Main Authors: Sumayah Saadi Abbas, Ammar A.Razzak Mahmood Kubba
Format: Article
Language:English
Published: College of Pharmacy University of Baghdad 2018-06-01
Series:Iraqi Journal of Pharmaceutical Sciences
Online Access:https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/712
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spelling doaj-2a497b1faf0c48099a1f8af613d2d1af2021-06-20T10:10:01ZengCollege of Pharmacy University of BaghdadIraqi Journal of Pharmaceutical Sciences2521-35121683-35972018-06-0127110.31351/vol27iss1pp69-78712Synthesis and antimicrobial evaluation with DFT study for new thiazole derivativesSumayah Saadi Abbas0Ammar A.Razzak Mahmood Kubbacollege of pharmacy\university of baghdad Two compounds,[2-amino-4-(4-nitro phenyl) 1,3-thiazole],(4) and [2-amino-4-(4-bromo phenyl) 1,3-thiazole],(5), were synthesized by refluxing thiourea (1) with each of  para-ntiro and para-bomophanacyl bromides(2) and (3) respectively, in absolute methanol. Then, by reaction of [5] with 3,5-dinitrobenzoyl chloride in dimethylformamide (DMF) yielded  (6) .On the other hand, reaction of (4) with chloroacetyl chloride in dry benzene afforded (7), which is  upon treatment with thiourea in absolute methanol, afforded (8) . The characterization of the titled compounds were done utilizing FTIR spectroscopy, 1HNMR, CHNS elemental analysis and by measurements of  their physical properties. The synthesized compounds had been screened for their, in vitro  preliminary antimicrobial activity against four Gram positive bacteria (Staph. aureus, Micrococcus luteus, Bacillus subtilis and Bacillus pumilus),  and four Gram negative bacteria (Pseud.aeroginosa, E.coli, Proteus mirabilis and Klebsiella pneumoniae)and three fungi species: (Saccharomyces cerevisiae, Candida Tropicalis and Candida albicans) using a minimum  inhibitory concentration (MIC) of 100 µg\ml of derivative  in dimethylsulfoxide, by  well diffusion method. Compound (6) showed moderate antibacterial activity against some tested Gram positive bacteria (Bacillus pumilus and Bacillus Subtilis) and a moderate antifungal activity towards Candida albicans. Computational study was performed   to calculate some of the thermodynamic parameters of synthesized derivatives by using density functional theory (DFT). https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/712
collection DOAJ
language English
format Article
sources DOAJ
author Sumayah Saadi Abbas
Ammar A.Razzak Mahmood Kubba
spellingShingle Sumayah Saadi Abbas
Ammar A.Razzak Mahmood Kubba
Synthesis and antimicrobial evaluation with DFT study for new thiazole derivatives
Iraqi Journal of Pharmaceutical Sciences
author_facet Sumayah Saadi Abbas
Ammar A.Razzak Mahmood Kubba
author_sort Sumayah Saadi Abbas
title Synthesis and antimicrobial evaluation with DFT study for new thiazole derivatives
title_short Synthesis and antimicrobial evaluation with DFT study for new thiazole derivatives
title_full Synthesis and antimicrobial evaluation with DFT study for new thiazole derivatives
title_fullStr Synthesis and antimicrobial evaluation with DFT study for new thiazole derivatives
title_full_unstemmed Synthesis and antimicrobial evaluation with DFT study for new thiazole derivatives
title_sort synthesis and antimicrobial evaluation with dft study for new thiazole derivatives
publisher College of Pharmacy University of Baghdad
series Iraqi Journal of Pharmaceutical Sciences
issn 2521-3512
1683-3597
publishDate 2018-06-01
description Two compounds,[2-amino-4-(4-nitro phenyl) 1,3-thiazole],(4) and [2-amino-4-(4-bromo phenyl) 1,3-thiazole],(5), were synthesized by refluxing thiourea (1) with each of  para-ntiro and para-bomophanacyl bromides(2) and (3) respectively, in absolute methanol. Then, by reaction of [5] with 3,5-dinitrobenzoyl chloride in dimethylformamide (DMF) yielded  (6) .On the other hand, reaction of (4) with chloroacetyl chloride in dry benzene afforded (7), which is  upon treatment with thiourea in absolute methanol, afforded (8) . The characterization of the titled compounds were done utilizing FTIR spectroscopy, 1HNMR, CHNS elemental analysis and by measurements of  their physical properties. The synthesized compounds had been screened for their, in vitro  preliminary antimicrobial activity against four Gram positive bacteria (Staph. aureus, Micrococcus luteus, Bacillus subtilis and Bacillus pumilus),  and four Gram negative bacteria (Pseud.aeroginosa, E.coli, Proteus mirabilis and Klebsiella pneumoniae)and three fungi species: (Saccharomyces cerevisiae, Candida Tropicalis and Candida albicans) using a minimum  inhibitory concentration (MIC) of 100 µg\ml of derivative  in dimethylsulfoxide, by  well diffusion method. Compound (6) showed moderate antibacterial activity against some tested Gram positive bacteria (Bacillus pumilus and Bacillus Subtilis) and a moderate antifungal activity towards Candida albicans. Computational study was performed   to calculate some of the thermodynamic parameters of synthesized derivatives by using density functional theory (DFT).
url https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/712
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